HPB Surgery, 1991, Vol. 4, pp 255-260Reprints available directly from the publisherPhotocopying permitted by license only
1991 Harwood Academic Publishers GmbHPrinted in the United Kingdom
SYMPTOMATIC GALLSTONES:
Management Options For The 1990s
J. TOOULIGastrointestinal Surgical Unit, Department of Surgery, Flinders Medical Centre,
Bedford Park, S.A., 5042 Adelaide, Australia
(Received 7 March 1991)
KEY WORDS: Gallstones, laparoscopic cholecystectomy, cholecystectomy, ESWL, dissolution, ultra-sonography
INTRODUCTION
At the recent annual meeting of the Internatioflal Hepatobiliary and PancreaticAssociation in Hong Kong the following panel was assembled with the aims ofdiscussing the efficacy of the various methods of treatment available for patientswith symptomatic gallstones. The panel comprised Drs S.K. Lam, G. Stevenson,T.K. Choi, G. Berci, E. Mack and F. Moody and it was Chaired by J. Toouli.
INCIDENCE AND SYMPTOMS
Gallstones occur commonly in Western countries. It has been estimated that duringnormal life expectancy, 22% of men and 33% of women have gallstones, and thatin 50% of cases these are symptomatic1. In the United States, for example, some 15million people may have gallstones, the stones becoming symptomatic in somethree million cases between the ages of 55-60 years. Half a million cholecystecto-mies are performed yearly to treat gallstones. The stones usually in Westernpatients are normally cholesterol stones or mixed stones. Black pigment stonesoccur less frequently. In Asia, cholesterol stones are much less common, and thepredominant types are brown pigment and mixed stones. Brown pigment stones areamorphous, soft, and muddy, and thus tend to break up readily; an importantfeature when lithotripsy is being considered as a form of therapy. The male tofemale ratio of Chinese patients with gallstones is about 2 to 1 as opposed to theratio of 1 to 3 generally seen in Western countries.The major symptom produced by gallstones is pain. Dyspepsia, flatulence or
nausea are symptoms which are not specific to gallstones. Available data indicatethat treatment of gallstones should only be considered once symptoms develop2’3.
Address correspondence to: James Toouli, Professor & Head of Unit, Gastrointestinal Surgical Unit,Department of Surgery, Flinders Medical Centre, Bedford Park, S.A., 5042 Adelaide, Australia
255
256 J. TOOULI
In patients with asymptomatic gallstones, only approximately 10-20% eventuallydevelop symptoms.
INVESTIGATION
Ultrasonography is the initial investigation used when cholelithiasis is suspected4, ithas a sensitivity and specificity which are both between 94-98%. Unlike oralcholecystography, which has comparable reliability, ultrasonography avoids expo-sure to radiation. Cholecystography should be used only when doubt remains afterultrasonography. Ultrasonography is useful in the diagnosis of acute cholecystitis inthat oedema of the gallbladder wall may be detected. However, the sensitivity andspecificity of this sign has yet to be precisely determined. If there is doubt about thediagnosis of cholecystitis, scintigraphy is used to determine cystic duct patency. Anobstructed cystic duct supports the diagnosis of acute cholecystitis.
In patients being evaluated for extracorporeal shock wave lithotripsy (ESWL) ordissolution therapy the oral cholecystogram is used to determine cystic ductpatency and size of the gallstones. CT scan evaluation of the gallstones has beenused recently to detect rings of calcium in the stone5. Such stones are resistant totreatment by ESWL or dissolution.
Following pancreatitis ultrasonography is the most appropriate investigation todetect gallbladder stones. However, to determine whether stones are present in thebile duct, endoscopic cholangio pancreatography (ERCP) is the most accurateinvestigation. Ultrasonography has a low sensitivity for detecting stones in the bileduct.
CHOLECYSTECTOMY
Cholecystectomy remains the "gold standard" for the treatment of gallstones. It hasan operative mortality of less than 0.2%, a low morbidity and the majority ofpatients are cured of their disease6. A small percentage of patients may developpost-cholecystectomy biliary problems due to persistant or recurrent stone disease,iatrogenic injury or motility disorders affecting the sphincter of Oddi.Once stones have passed from the gallbladder into the bile duct the treatment
options depend on the patients age and the presence of associated medicalconditions. In patients without a gallbladder the preferred treatment for gallstonesin the bile duct is endoscopic sphincterotomy with extraction of the stones by abasket or balloon catheter. In patients with a gallbladder, choledochotomy at thetime of cholecystectomy is a safe procedure with low morbidity8. However inelderly or infirm patients, endoscopic sphincterectomy is recommended to extractthe bile duct stones leaving the gallbladder in situ. The overall incidence ofproblems arising from the retained gallbladder is approximately 15%; if the cysticduct is obstructed this incidence rises to around 50%
LAPAROSCOPIC CHOLECYSTECTOMY
Laparoscopic Cholecystectomy has created great interest since its recent introduc-tion. Series with large numbers of patients are being reported from France1, the
SYMPTOMATIC GALLSTONES 257
USA11 and Britain12. What is intriguing is the fact that patients are ambulant on theday after the procedure, with rapid discharge from hospital and a return to normalactivity, including work, within a week. On initial assessment there appear to beenormous advantages in carrying out cholecystectomy by laparoscopic means.Morbidity and mortality appear to be similar to that of open cholecystectomy1.The principles of the operation are identical to those for open surgery andprecautions to avoid iatrogenic injury need to be observed meticulously. As withany new procedure, training is vital for surgeons embarking on this type of surgery.In the opinion of many hepatobiliary surgeons, the laparoscopic approach to thebiliary tract will revolutionize surgery of the biliary tract. It .is estimated thatapproximately 70% of patients with symptomatic gallstones can be treated in thisway12. It is recommended at this stage that patients with acute cholecystitis shouldstill be treated by open cholecystectomy. Similarly, patients who have previouslyundergone surgery to the upper abdomen should be excluded as adhesions maymake laparoscopy hazardous. However future developments in laparoscopic tech-niques may reduce some of the contraindications and allow treatment of morepatients with symptomatic gallstones.
DISSOLUTION OF GALLSTONES
A variety of agents have been used to dissolve gallstones. The attraction of theseagents for patients with symptomatic gallstones and their clinicians is the possibilityof treating the stones without major intervention. However the fact that thegallbladder remains is often associated with significant recurrence of the gallstonesand the need for repeated treatment.Agents for oral dissolution include ursodiol (ursodeoxycholic acid, UDCA),
chenodiol (chenodeoxycholic acid CDCA) and terpenes (mainly menthol). Theseagents can be used alone or as adjuvant therapy. They can only be used for thetreatment of radiolucent cholesterol gallstones and require the presence of a patentcystic duct. CDCA acts by expanding the bile acid pool and inhibits cholesterolsynthesis and secretion. Diarrhoea, which is dose related, affects approximately50% of patients. CDCA leads to an increase in serum cholesterol as well astransient increase in serum amino transferases. The dose of CDCA is 15mg/kg/dayand the efficacy of dissolution is approximately 30-40% 13. The duration of oral bileacid therapy for dissolution is 1-2 years and the cost is approximately $US1.00/day.UDCA acts by inhibiting cholesterol secretion in bile and reduces gut cholesterol
absorption. It promotes non-micellar mechanisms of cholesterol solubilization andhas practically no side effects. The dosage of UDCA is 10mg/kg/day and theefficacy of dissolution for cholesterol gallstones is 50-80%. Duration of therapy isapproximately 1-2 years and the cost of the medication is $US3-4.00/day13.
Contact solvents used to dissolve cholesterol gallstones include mono-octanoin,methyltert-butyl ether (MTBE), D-limonene, GS-100, and EDTA. Mono-octanoinhas been used more extensively, mainly for dissolving stones in the bile duct. Sideeffects include nausea, vomiting, pain and diarrhoea. The efficacy for dissolution ofbile duct stones is 50-80% following continuous infusion into the bile duct for up to1 week.MTBE is an experimental agent which is mainly employed for cholesterol stones
within the gallbladder. It is explosive and malodorous and it causes nausea andoverflow sedation, as well as duodenitis. The duration of treatment for gallstone
258 J. TOOULI
dissolution is 1-3 days and efficacy is 90-100%. EDTA-bile acid mixtures havebeen used experimentally for brown pigment stones. The disadvantages are again aslow dissolution rate and an adjuvant agent or technique is needed for successfuloutcomeTM.The major disadvantage of all dissolution agents is the recurrence rate which for
CDCA and UDCA is recorded at 50% at 5 years. However in patients deemed tobe at major risk following more invasive procedures, dissolution therapy provides aminimally invasive avenue for therapy. The indications to use mono-octanoin totreat bile duct stones have diminished with the availability of endoscopic andpercutaneous methods of stone extraction. However occasionally it may be used asan adjuvant to the extraction technique in order to soften or reduce the size of alarge stone so that it might more easily be removed15.
EXTRACORPOREAL SHOCK WAVE LITHOTRIPSY
Non interventional treatment of gallstones appeared to become reality with the firstreports of extracorporeal shock wave lithotripsy (ESWL) in the treatment ofsymptomatic gallstones16. Results from a trial conducted in Munich using a waterbath spark-gap acoustic generator reported efficacy of approximately 90% inappropriate patients maintained on chenodiol and ursodiol for one year afterlithotripsy. On the basis of this experience trials were initiated using three types ofacoustical wave generators; spark-gap, electromagnetic and piezo electric. Thespark gap generator has a broader acoustical focus at the level of the target zoneand therefore has a greater success at shattering the stones. However it requiresanalgesia and sedation during treatments. The electromagnetic and piezo electricmachines offer relatively pain-free treatment but multiple treatments because oftheir small focal zone. All of the techniques require adjuvant bile salt therapy forapproximately one year to obtain stone clearance.Experience in subsequent trials, conducted mainly in the USA have provided the
following principles. ESWL is safe and well tolerated. Selection and targetting areessential for success. The fragmentation rate is approximately 90% in patients withnon-calcified stones. Approximately 40% of patients have biliary colic in the earlyweeks after treatment. Thirty per cent will have stone fragments of a size that willbenefit from retreatment. Approximately 10% of patients require cholecystectomyfor continuing symptoms and all patients require bile salt therapy to achieve stoneclearance. The overall success rate for stone clearance at 6 months is between 42and 69%, but this may improve up to 90% at one year19. A major drawback is therecurrence rate after successful dissolution. Early reports suggest a recurrence rateof stones of approximately 10% per year and is similar to the recurrence ratereported after either UDCA or CDCA therapy21.
RECOMMENDATIONS
The panel concluded that symptomatic gallstones, as opposed to asymptomaticstones, warrant treatment. The initial investigation to demonstrate gallstones isultrasonography and in the majority of patients, this investigation suffices prior to
SYMPTOMATIC GALLSTONES 259
treatment. Cholecystectomy is the most efficacious therapy for symptomatic gall-stones in most patients. With the evolution of laparoscopic cholecystectomy and itsattributes, this technique is poised to become the gold standard for the treatment ofgallstones. In patients with stones in the bile duct presenting some time aftercholecystectomy and demonstrated by ERCP, extraction after endoscopic sphinc-terotomy provides the best approach. All other techniques for the management ofgallstones are either inferior to the above or are experimental and recommendedonly for specific clinical situations which do not allow the use of the abovetechniques. Dissolution therapy using oral agents or contact solutions are confinedto patients with medical disorders which make the above procedures hazardous.ESWL is used as an aid to dissolution. However its overall efficacy requires furtherstudy. The major drawback for both dissolution and ESWL is the high recurrenceof gallstones whereas cholecystectomy by laparoscopic means or open surgery dealswith the diseased gallbladder permanently.
References1. McSherry, C.K., Ferstenberg, H., Calhoun, W.F., Lahmana, E. and Virshup, M. (1985) The
natural history of diagnosed gallstone disease in symptomatic and asymptomatic patients. Ann.Surg., 202, 59-63
2. Ransohoff, D.F., Gracie, W.A., Wolfenson, L.B. and Neuhauser, D. (1983) Prophylacticcholecystectomy or expectant management for silent gallstones. A decision analysis to assesssurvival. Annals of Internal Medicine, 99, 199-204
3. Rome Group for the epidemiology and prevention of cholelithiasis (GREPCO) (1984) Prevalenceof gallstones disease in an Italian adult female population. Americaa Journal of Epidemiology,119,796-805
4. Bartrum, R.J. Jr, Crow, H.C. and Foote, S.R. (1977) Ultrasonic and radiographic cholecystogra-phy. New England Journal of Medicine, 2911, 538-541
5. Brakel, J., Lameris, J.S., Nijs, H.G.T., Terpstra, O.T., Steen, G. and Blijenberg, B.C. (1990)Predicting gallstone composition with CTL: in vivo and in vitro analysis. Radiology, 174, 337-341
6. McSherry, C.K. and Glenn, F. (1980) The incidence and causes of death following surgery for non-malignant biliary tract disease. Annals of Surgery, 191,271-275
7. Cotton, P.B. (1984) Endoscopic management of bile duct disorders; (apples and oranges). Gut, 25,587-597
8. Worthley, C.S., Watts, J.McK. and Toouli, J. (1989) Common duct exploration or endoscopicsphincterotomy for choledocholithiasis. ANZ Journal of Surgery, 59, 209-216
9. Worthley, C.S. and Toouli, J. (1989) Gallbladder non-filling: an indication for cholecystectomyfollowing endoscopic sphincterotomy. Br. J. Surg., 75, 796-798
10. Dubois, F., Berthelot, G. and Levard, H. (1989) Cholecystectomie par Coelioscopie. Presse Med.,18, 980-982
11. Reddick, E.J. and Olsen, D.O. (1989) Laparoscopic laser cholecystectomy. A comparison withmini-lap cholecystectomy. Surg. Endosc., 3, 131-133
12. Cushieri, A., Berci, G. and McSherry, C.K. (1990) Laparoscopic Cholecystectomy. Amer. J.Surg., 159, 273
13. Hofmann, A.F. (1989) Medical dissolution of gallstones by oral bile acid therapy. Amer. J. Surg.,158, 198-204
14. Mack, E. (1986) Chemical dissolution of biliary stones. Contemp. Surg., 28, 20-2315. Mack, E. (1990) Role of surgery in the management of gallstones. Seminars in Liver Disease, 10,
222-23116. Sauerbruch, T., Delius, M., Paumgartner, G. et al. (1986) Fragmentation of gallstones by
extracorporeal shock waves. N. Eng. J. Med., 314, 822-82817. Sackmann, M., Delius, M., Sauerbruch T. et al. (1988) Shock wave lithotripsy of gallbladder
stones. N. Engl. J., Med., 318, 393-39718. Albert, M.B. and Fromm, H. (1990) US Multicenter study of the safety and efficacy in treating
gallstones with Piezoelectric lithotripsy. Gastroenterology, 98, Part 2 A564
260 J. TOOULI
19. Burnett, D., Ertan, A. and Jones, R. (1989) Use of external shockwave lithotripsy and adjuvantursodiol for treatment of radiolucent gallstones. A national multicenter study. Dig. Dis. Sci., 34,1011-1015
20. Darzi, A., EI-Sayed, E., Tanner, W.A. and Keane, F.B.V. (1990) Gallstone recurrence aftersuccessful shock wave lithotripsy. Gastroenterology, 98, Part 2 A580
21. Villanova, N., Bazzoli, F., Taroni, F., Frabboni, R., Mdzzella, G., Fresti, D., Barbara, L. andRoda, E. (1989) Gallstone recurrence after successful bile acid treatment. A 12 year follow-upstudy and evaluation of longterm post-dissolution treatment. Gastroenterology, 97,726-731
(On invitation by S. Bengmark, received 7 March 1991)
Submit your manuscripts athttp://www.hindawi.com
Stem CellsInternational
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
MEDIATORSINFLAMMATION
of
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
Behavioural Neurology
EndocrinologyInternational Journal of
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
Disease Markers
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
BioMed Research International
OncologyJournal of
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
Oxidative Medicine and Cellular Longevity
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
PPAR Research
The Scientific World JournalHindawi Publishing Corporation http://www.hindawi.com Volume 2014
Immunology ResearchHindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
Journal of
ObesityJournal of
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
Computational and Mathematical Methods in Medicine
OphthalmologyJournal of
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
Diabetes ResearchJournal of
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
Research and TreatmentAIDS
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
Gastroenterology Research and Practice
Hindawi Publishing Corporationhttp://www.hindawi.com Volume 2014
Parkinson’s Disease
Evidence-Based Complementary and Alternative Medicine
Volume 2014Hindawi Publishing Corporationhttp://www.hindawi.com